A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515844



Internal ID15442901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:777799..787095hg38UCSC Ensembl
Innerchr4:771587..780883hg19UCSC Ensembl
Innerchr4:761587..770883hg18UCSC Ensembl
Innerchr4:761417..770713hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg389297
hg199297
hg189297
hg179297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664993, nssv661696
Samples
Known GenesCPLX1, LOC100129917
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515844
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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