A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3745476



Internal ID18697071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:37865815..38187846hg38UCSC Ensembl
Innerchr6:37833591..38155622hg19UCSC Ensembl
Innerchr6:37941569..38263600hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38322032
hg19322032
hg18322032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020625
Supporting Variants
Samples
Known GenesBTBD9, ZFAND3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3745476
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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