A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526825



Internal ID15107432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:139442337..139483870hg38UCSC Ensembl
Innerchr7:139127083..139168616hg19UCSC Ensembl
Innerchr7:138777623..138819156hg18UCSC Ensembl
Innerchr7:138584338..138625871hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3841534
hg1941534
hg1841534
hg1741534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703181
Samples
Known GenesKLRG2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526825
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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