A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065864



Internal ID19155083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46192180..46276519hg38UCSC Ensembl
Innerchr17:44269546..44353885hg19UCSC Ensembl
Innerchr17:41625323..41709662hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3884340
hg1984340
hg1884340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3237n100
Supporting Variantsnssv3557429
Samples
Known GenesKANSL1, KANSL1-AS1, LOC644172
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065864
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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