A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063039



Internal ID18805570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2873325..2917578hg38UCSC Ensembl
Innerchr19:2873323..2917576hg19UCSC Ensembl
Innerchr19:2824323..2868576hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3844254
hg1944254
hg1844254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564604
Samples
Known GenesZNF556, ZNF57
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063039
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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