A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654998



Internal ID15044964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:32844072..32879164hg38UCSC Ensembl
Innerchr19:33334978..33370070hg19UCSC Ensembl
Innerchr19:38026818..38061910hg18UCSC Ensembl
Innerchr19:38026818..38061910hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3835093
hg1935093
hg1835093
hg1735093
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516922
Supporting Variants
Samples
Known GenesCEP89, SLC7A9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654998
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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