A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691302



Internal ID18989583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:112930003..112980131hg38UCSC Ensembl
Innerchr8:113942232..113992360hg19UCSC Ensembl
Innerchr8:114011408..114061536hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3850129
hg1950129
hg1850129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030305
Supporting Variants
Samples
Known GenesCSMD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691302
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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