A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705544



Internal ID15442196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:24649594..24724181hg38UCSC Ensembl
Innerchr2:24872463..24947050hg19UCSC Ensembl
Innerchr2:24725967..24800554hg18UCSC Ensembl
Innerchr2:24784114..24858701hg17UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3874588
hg1974588
hg1874588
hg1774588
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528864
Supporting Variants
Samples
Known GenesNCOA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705544
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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