A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6977957



Internal ID12631706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46080231..46190497hg38UCSC Ensembl
Innerchr17:44157597..44267863hg19UCSC Ensembl
Innerchr17:41513416..41623640hg18UCSC Ensembl
Innerchr17:41513416..41623640hg17UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38110267
hg19110267
hg18110225
hg17110225
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751704
Supporting Variants
SamplesNA10847
Known GenesKANSL1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6977957
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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