A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704948



Internal ID15094914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56127476..56177201hg38UCSC Ensembl
Innerchr19:56638845..56688570hg19UCSC Ensembl
Innerchr19:61330657..61380382hg18UCSC Ensembl
Innerchr19:61330657..61380382hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3849726
hg1949726
hg1849726
hg1749726
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528361
Supporting Variants
Samples
Known GenesGALP, ZNF444
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704948
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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