A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699368



Internal ID15089334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162602818..162615479hg38UCSC Ensembl
Innerchr6:163023850..163036511hg19UCSC Ensembl
Innerchr6:162943840..162956501hg18UCSC Ensembl
Innerchr6:162994261..163006922hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3812662
hg1912662
hg1812662
hg1712662
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)nssv699368
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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