A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567532



Internal ID18865813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41470743..41517216hg38UCSC Ensembl
Innerchr19:41976648..42023588hg19UCSC Ensembl
Innerchr19:46668488..46715428hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3846474
hg1946941
hg1846941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057764
Supporting Variants
Samples
Known GenesLOC100505495
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3567532
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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