A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684607



Internal ID15421259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11857464..11905556hg38UCSC Ensembl
Innerchr9:11857464..11905556hg19UCSC Ensembl
Innerchr9:11847464..11895556hg18UCSC Ensembl
Innerchr9:11847464..11895556hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3848093
hg1948093
hg1848093
hg1748093
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517379
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684607
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