A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564706



Internal ID18862987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12387780..12434058hg38UCSC Ensembl
Innerchr19:12498594..12544872hg19UCSC Ensembl
Innerchr19:12359594..12405872hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3846279
hg1946279
hg1846279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061424
Supporting Variants
Samples
Known GenesZNF443, ZNF799
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564706
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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