A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657455



Internal ID18955736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:51307201..51332673hg38UCSC Ensembl
Innerchr6:51171999..51197471hg19UCSC Ensembl
Innerchr6:51279958..51305430hg18UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3825473
hg1925473
hg1825473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031270
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3657455
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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