A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564677



Internal ID18862958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8685780..8710502hg38UCSC Ensembl
Innerchr19:8796030..8820855hg19UCSC Ensembl
Innerchr19:8657030..8681855hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3824723
hg1924826
hg1824826
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065034
Supporting Variants
Samples
Known GenesACTL9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564677
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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