A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568149



Internal ID18866430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35364439..35375872hg38UCSC Ensembl
Innerchr19:35855341..35866774hg19UCSC Ensembl
Innerchr19:40547181..40558614hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3811434
hg1911434
hg1811434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065109
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)nssv3568149
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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