A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697867



Internal ID15087833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:516350..518078hg38UCSC Ensembl
Innerchr6:516350..518078hg19UCSC Ensembl
Innerchr6:461350..463078hg18UCSC Ensembl
Innerchr6:461350..463078hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381729
hg191729
hg181729
hg171729
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521248
Supporting Variants
Samples
Known GenesEXOC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697867
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