A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685361



Internal ID18983642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:21939585..21974708hg38UCSC Ensembl
Innerchr8:21797096..21832219hg19UCSC Ensembl
Innerchr8:21853042..21888165hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3835124
hg1935124
hg1835124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034335
Supporting Variants
Samples
Known GenesXPO7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3685361
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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