A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522075



Internal ID15102682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:25224281..25224937hg38UCSC Ensembl
Innerchr7:25263900..25264556hg19UCSC Ensembl
Innerchr7:25230425..25231081hg18UCSC Ensembl
Innerchr7:25037140..25037796hg17UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38657
hg19657
hg18657
hg17657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694846
Samples
Known GenesNPVF
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522075
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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