A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700682



Internal ID15090648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:137169614..137176295hg38UCSC Ensembl
Innerchr4:138090768..138097449hg19UCSC Ensembl
Innerchr4:138310218..138316899hg18UCSC Ensembl
Innerchr4:138448373..138455054hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg386682
hg196682
hg186682
hg176682
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516176
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700682
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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