A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694085



Internal ID15430737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:105521361..105527743hg38UCSC Ensembl
Innerchr4:106442518..106448900hg19UCSC Ensembl
Innerchr4:106661967..106668349hg18UCSC Ensembl
Innerchr4:106800122..106806504hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg386383
hg196383
hg186383
hg176383
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521423
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694085
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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