A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061424



Internal ID19150643
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 StatusM
Merged Variantsdgv3431n100
Supporting Variantsnssv3564706
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)nsv1061424
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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