A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517519



Internal ID15444812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:63318964..63349197hg38UCSC Ensembl
Innerchr4:64184682..64214915hg19UCSC Ensembl
Innerchr4:63867277..63897510hg18UCSC Ensembl
Innerchr4:64013448..64043681hg17UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3830234
hg1930234
hg1830234
hg1730234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688583, nssv667715, nssv677950, nssv660479, nssv688557, nssv671877, nssv655758, nssv654783, nssv671402, nssv663403, nssv652256, nssv674174, nssv690921, nssv688347, nssv680204, nssv684200, nssv665308, nssv685127, nssv688974, nssv683196, nssv677511, nssv681103, nssv690501, nssv674391, nssv683147, nssv674101, nssv680843, nssv682181
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517519
Frequency
Sample Size2026
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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