A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757486



Internal ID19055767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675630..136849940hg38UCSC Ensembl
Innerchr8:137687873..137862183hg19UCSC Ensembl
Innerchr8:137757055..137931365hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38174311
hg19174311
hg18174311
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015463
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)nssv3757486
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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