A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518997



Internal ID15446290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:36763358..36767776hg38UCSC Ensembl
Innerchr7:36802963..36807381hg19UCSC Ensembl
Innerchr7:36769488..36773906hg18UCSC Ensembl
Innerchr7:36576203..36580621hg17UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg384419
hg194419
hg184419
hg174419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696464
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518997
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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