A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515778



Internal ID15442835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:42504120..42507401hg38UCSC Ensembl
Innerchr7:42543719..42547000hg19UCSC Ensembl
Innerchr7:42510244..42513525hg18UCSC Ensembl
Innerchr7:42316959..42320240hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg383282
hg193282
hg183282
hg173282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664747, nssv662477
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515778
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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