A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685549



Internal ID18637144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:28763136..28821165hg38UCSC Ensembl
Innerchr8:28620653..28678682hg19UCSC Ensembl
Innerchr8:28676572..28734601hg18UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3858030
hg1958030
hg1858030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032475
Supporting Variants
Samples
Known GenesINTS9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3685549
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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