A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515871



Internal ID15442928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:58630658..58631756hg38UCSC Ensembl
Innerchr17:56708019..56709117hg19UCSC Ensembl
Innerchr17:54063018..54064116hg18UCSC Ensembl
Innerchr17:54063018..54064116hg17UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381099
hg191099
hg181099
hg171099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669356, nssv657965, nssv670312, nssv693495, nssv663522, nssv686353, nssv655966, nssv698322, nssv687693, nssv672897, nssv661384, nssv665096
Samples
Known GenesTEX14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515871
Frequency
Sample Size2026
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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