A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3573774



Internal ID18872055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43414688..43450763hg38UCSC Ensembl
Innerchr19:43918840..43954915hg19UCSC Ensembl
Innerchr19:48610680..48646755hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3836076
hg1936076
hg1836076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066231
Supporting Variants
Samples
Known GenesTEX101
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3573774
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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