A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685992



Internal ID18984273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39441317..39505415hg38UCSC Ensembl
Innerchr8:39298836..39362934hg19UCSC Ensembl
Innerchr8:39417993..39482091hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3864099
hg1964099
hg1864099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027002
Supporting Variants
Samples
Known GenesADAM3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3685992
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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