A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515738



Internal ID15442795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:50408411..50426509hg38UCSC Ensembl
Innerchr7:50476109..50494207hg19UCSC Ensembl
Innerchr7:50443603..50461701hg18UCSC Ensembl
Innerchr7:50250318..50268416hg17UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3818099
hg1918099
hg1818099
hg1718099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686093, nssv663178, nssv676346, nssv656256, nssv667884, nssv664638
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515738
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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