A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527833



Internal ID15455126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12592460..12604877hg38UCSC Ensembl
Innerchr7:12632085..12644502hg19UCSC Ensembl
Innerchr7:12598610..12611027hg18UCSC Ensembl
Innerchr7:12405325..12417742hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3812418
hg1912418
hg1812418
hg1712418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704329
Samples
Known GenesSCIN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527833
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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