A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517156



Internal ID15444449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37940970..37944758hg38UCSC Ensembl
Innerchr3:37982461..37986249hg19UCSC Ensembl
Innerchr3:37957465..37961253hg18UCSC Ensembl
Innerchr3:37957465..37961253hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg383789
hg193789
hg183789
hg173789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv654361, nssv690647, nssv660492, nssv692675, nssv688865, nssv686919, nssv673225, nssv655454, nssv678461, nssv693996, nssv670075, nssv687246, nssv693608, nssv664531, nssv668775, nssv654245, nssv693641, nssv656733, nssv684625, nssv657669, nssv668957, nssv659370, nssv657776, nssv673282, nssv659133, nssv661154, nssv677067, nssv659249, nssv683264, nssv669068, nssv682963, nssv660252, nssv669904, nssv686361, nssv654848, nssv690999, nssv670694, nssv668704, nssv675858, nssv692430, nssv659597, nssv688581, nssv652252, nssv672534, nssv653889, nssv691356, nssv686684, nssv667882, nssv676158, nssv652777, nssv675472, nssv675508, nssv664633, nssv663968, nssv658788, nssv690512, nssv669852, nssv681288, nssv657552, nssv667730, nssv689184, nssv680800, nssv663604, nssv672379, nssv692407, nssv660401, nssv676555, nssv672160
Samples
Known GenesCTDSPL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517156
Frequency
Sample Size2026
Observed Gain0
Observed Loss68
Observed Complex0
Frequencyn/a


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