A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701984



Internal ID15438636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103480929..103484808hg38UCSC Ensembl
Innerchr10:105240686..105244565hg19UCSC Ensembl
Innerchr10:105230676..105234555hg18UCSC Ensembl
Innerchr10:105230676..105234555hg17UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg383880
hg193880
hg183880
hg173880
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525801
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701984
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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