A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749019



Internal ID19047300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:8592266..8718879hg38UCSC Ensembl
Innerchr6:8592499..8719112hg19UCSC Ensembl
Innerchr6:8537498..8664111hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38126614
hg19126614
hg18126614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022625
Supporting Variants
Samples
Known GenesHULC, LOC100506207
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3749019
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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