A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701664



Internal ID15438316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:83530727..83576787hg38UCSC Ensembl
Innerchr3:83579878..83625938hg19UCSC Ensembl
Innerchr3:83662568..83708628hg18UCSC Ensembl
Innerchr3:83662568..83708628hg17UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3846061
hg1946061
hg1846061
hg1746061
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525529
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701664
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