A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691330



Internal ID18989611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114589534..114629490hg38UCSC Ensembl
Innerchr8:115601763..115641719hg19UCSC Ensembl
Innerchr8:115670939..115710895hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3839957
hg1939957
hg1839957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015198
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)nssv3691330
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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