A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657495



Internal ID18955776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:55500671..55511532hg38UCSC Ensembl
Innerchr6:55365469..55376330hg19UCSC Ensembl
Innerchr6:55473428..55484289hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3810862
hg1910862
hg1810862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020349
Supporting Variants
Samples
Known GenesHMGCLL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3657495
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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