A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065163



Internal ID19154382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20833577..20875004hg38UCSC Ensembl
Innerchr17:20736890..20778317hg19UCSC Ensembl
Innerchr17:20677482..20718909hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3841428
hg1941428
hg1841428
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3122n100
Supporting Variantsnssv3560920
Samples
Known GenesCCDC144NL, LOC440416
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065163
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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