A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3747901



Internal ID19046182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:3164884..3223279hg38UCSC Ensembl
Innerchr6:3165118..3223513hg19UCSC Ensembl
Innerchr6:3110117..3168512hg18UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3858396
hg1958396
hg1858396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026561
Supporting Variants
Samples
Known GenesLOC100507194
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3747901
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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