A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694040



Internal ID15084006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162374026..162420947hg38UCSC Ensembl
Innerchr6:162795058..162841979hg19UCSC Ensembl
Innerchr6:162715048..162761969hg18UCSC Ensembl
Innerchr6:162765469..162812390hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3846922
hg1946922
hg1846922
hg1746922
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517562
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694040
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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