A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523744



Internal ID15451037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61089312..62376223hg38UCSC Ensembl
Innerchr7:61072037..61852895hg19UCSC Ensembl
Innerchr7:61075979..61490330hg18UCSC Ensembl
Innerchr7:60882694..61297045hg17UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381286912
hg19780859
hg18414352
hg17414352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699560
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523744
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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