A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703482



Internal ID15093448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:140437078..140451331hg38UCSC Ensembl
Innerchr4:141358232..141372485hg19UCSC Ensembl
Innerchr4:141577682..141591935hg18UCSC Ensembl
Innerchr4:141715837..141730090hg17UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3814254
hg1914254
hg1814254
hg1714254
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527102
Supporting Variants
Samples
Known GenesLOC152586
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703482
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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