A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564604



Internal ID18516199
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 StatusS
Merged Variantsnsv1063039
Supporting Variants
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)nssv3564604
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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