A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691319



Internal ID18989600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114241276..114280691hg38UCSC Ensembl
Innerchr8:115253505..115292920hg19UCSC Ensembl
Innerchr8:115322681..115362096hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3839416
hg1939416
hg1839416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033038
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)nssv3691319
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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