A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689734



Internal ID18988015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:95435005..95450433hg38UCSC Ensembl
Innerchr8:96447233..96462661hg19UCSC Ensembl
Innerchr8:96516409..96531837hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3815429
hg1915429
hg1815429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021951
Supporting Variants
Samples
Known GenesLOC100616530
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689734
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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