A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688559



Internal ID15425211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100420903..100456312hg38UCSC Ensembl
Innerchr6:100868779..100904188hg19UCSC Ensembl
Innerchr6:100975500..101010909hg18UCSC Ensembl
Innerchr6:100975500..101010909hg17UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3835410
hg1935410
hg1835410
hg1735410
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515895
Supporting Variants
Samples
Known GenesSIM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688559
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