A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515924



Internal ID15442981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:36902513..36929802hg38UCSC Ensembl
Innerchr4:36904135..36931424hg19UCSC Ensembl
Innerchr4:36580530..36607819hg18UCSC Ensembl
Innerchr4:36726701..36753990hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3827290
hg1927290
hg1827290
hg1727290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv687013, nssv677309, nssv654868, nssv691235, nssv661255, nssv665321, nssv679905, nssv703771, nssv665653, nssv698335, nssv675584, nssv672684
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515924
Frequency
Sample Size2026
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer