A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705781



Internal ID15095747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14046247..14047978hg38UCSC Ensembl
Innerchr8:13903756..13905487hg19UCSC Ensembl
Innerchr8:13948127..13949858hg18UCSC Ensembl
Innerchr8:13948127..13949858hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381732
hg191732
hg181732
hg171732
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517019
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705781
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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