A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759778



Internal ID19058059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:78594550..78639074hg38UCSC Ensembl
Innerchr9:81209466..81253990hg19UCSC Ensembl
Innerchr9:80399286..80443810hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3844525
hg1944525
hg1844525
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045321
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)nssv3759778
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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