A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528448



Internal ID15455741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:119093361..119104396hg38UCSC Ensembl
Innerchr7:118733415..118744450hg19UCSC Ensembl
Innerchr7:118520651..118531686hg18UCSC Ensembl
Innerchr7:118327366..118338401hg17UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3811036
hg1911036
hg1811036
hg1711036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705047
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528448
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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