A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061158



Internal ID19150377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41251729..41274267hg38UCSC Ensembl
Innerchr17:39407981..39430519hg19UCSC Ensembl
Innerchr17:36661507..36684045hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3822539
hg1922539
hg1822539
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3160n100
Supporting Variantsnssv3720862, nssv3562586, nssv3562591, nssv3562592, nssv3720861, nssv3562587, nssv3562588, nssv3562590, nssv3562589
Samples
Known GenesKRTAP9-6, KRTAP9-9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061158
Frequency
Sample Size11257
Observed Gain4
Observed Loss5
Observed Complex0
Frequencyn/a


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