A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515912



Internal ID15442969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:40281265..40283721hg38UCSC Ensembl
Innerchr4:40282885..40285341hg19UCSC Ensembl
Innerchr4:39959280..39961736hg18UCSC Ensembl
Innerchr4:40105451..40107907hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382457
hg192457
hg182457
hg172457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665274, nssv673316, nssv685104
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515912
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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