A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522250



Internal ID15449543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:50375028..50387038hg38UCSC Ensembl
Innerchr7:50442726..50454736hg19UCSC Ensembl
Innerchr7:50410220..50422230hg18UCSC Ensembl
Innerchr7:50216935..50228945hg17UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3812011
hg1912011
hg1812011
hg1712011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695031
Samples
Known GenesIKZF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522250
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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