A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028500



Internal ID19117718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:21939585..21975988hg38UCSC Ensembl
Innerchr8:21797096..21833499hg19UCSC Ensembl
Innerchr8:21853042..21889445hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3836404
hg1936404
hg1836404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7135n100
Supporting Variantsnssv3685362
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)nsv1028500
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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