A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3680644



Internal ID18978925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7534398..7598490hg38UCSC Ensembl
Innerchr8:7391920..7456012hg19UCSC Ensembl
Innerchr8:7379330..7443422hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3864093
hg1964093
hg1864093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030537
Supporting Variants
Samples
Known GenesFAM90A7P, PRR23D1, PRR23D2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3680644
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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