A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672625



Internal ID15062591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56080920..56158389hg38UCSC Ensembl
Innerchr19:56592286..56669758hg19UCSC Ensembl
Innerchr19:61284098..61361570hg18UCSC Ensembl
Innerchr19:61284098..61361570hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3877470
hg1977473
hg1877473
hg1777473
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517365
Supporting Variants
Samples
Known GenesZNF444, ZNF787
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672625
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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