A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658229



Internal ID15394881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:5455411..5456919hg38UCSC Ensembl
Innerchr19:5455422..5456930hg19UCSC Ensembl
Innerchr19:5406422..5407930hg18UCSC Ensembl
Innerchr19:5406422..5407930hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381509
hg191509
hg181509
hg171509
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516923
Supporting Variants
Samples
Known GenesZNRF4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658229
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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