A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523632



Internal ID15450925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:122114641..122162014hg38UCSC Ensembl
Innerchr7:121754695..121802068hg19UCSC Ensembl
Innerchr7:121541931..121589304hg18UCSC Ensembl
Innerchr7:121348646..121396019hg17UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3847374
hg1947374
hg1847374
hg1747374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699432
Samples
Known GenesAASS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523632
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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