A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704127



Internal ID15440779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39983318..40046132hg38UCSC Ensembl
Innerchr4:39984938..40047752hg19UCSC Ensembl
Innerchr4:39661333..39724147hg18UCSC Ensembl
Innerchr4:39807504..39870318hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3862815
hg1962815
hg1862815
hg1762815
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527656
Supporting Variants
Samples
Known GenesLOC344967
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704127
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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