A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517155



Internal ID15097762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151792469..151828253hg38UCSC Ensembl
Innerchr3:151510257..151546041hg19UCSC Ensembl
Innerchr3:152992947..153028731hg18UCSC Ensembl
Innerchr3:152992955..153028739hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3835785
hg1935785
hg1835785
hg1735785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665692, nssv670027, nssv665549, nssv660490, nssv658351, nssv653926, nssv668991, nssv653888, nssv659090, nssv656462, nssv679762, nssv663926, nssv670149, nssv682732, nssv678031, nssv658456, nssv681567, nssv665336, nssv680976, nssv685121, nssv684424, nssv653372, nssv663219, nssv682151, nssv667901, nssv662629, nssv654575, nssv682205, nssv662124, nssv678327, nssv674220, nssv663106, nssv693150
Samples
Known GenesAADAC, MIR548H2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517155
Frequency
Sample Size2026
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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