A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704901



Internal ID15441553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:164888162..164906597hg38UCSC Ensembl
Innerchr4:165809314..165827749hg19UCSC Ensembl
Innerchr4:166028764..166047199hg18UCSC Ensembl
Innerchr4:166166919..166185354hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3818436
hg1918436
hg1818436
hg1718436
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528320
Supporting Variants
Samples
Known GenesLOC100506013
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704901
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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