A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655888



Internal ID15392540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75379524..75598736hg38UCSC Ensembl
Innerchr3:75428675..75647887hg19UCSC Ensembl
Innerchr3:75511365..75730577hg18UCSC Ensembl
Innerchr3:75511365..75730577hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38219213
hg19219213
hg18219213
hg17219213
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517173
Supporting Variants
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655888
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