A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702123



Internal ID15438775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:127841247..127841783hg38UCSC Ensembl
Innerchr6:128162392..128162928hg19UCSC Ensembl
Innerchr6:128204085..128204621hg18UCSC Ensembl
Innerchr6:128204085..128204621hg17UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38537
hg19537
hg18537
hg17537
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525919
Supporting Variants
Samples
Known GenesTHEMIS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702123
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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