A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701194



Internal ID15091160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:5055185..5059349hg38UCSC Ensembl
Innerchr19:5055196..5059360hg19UCSC Ensembl
Innerchr19:5006196..5010360hg18UCSC Ensembl
Innerchr19:5006196..5010360hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384165
hg194165
hg184165
hg174165
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525126
Supporting Variants
Samples
Known GenesKDM4B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701194
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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