A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757300



Internal ID19055581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:80378152..80416758hg38UCSC Ensembl
Innerchr8:81290387..81328993hg19UCSC Ensembl
Innerchr8:81452942..81491548hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3838607
hg1938607
hg1838607
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031421
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)nssv3757300
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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