A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699285



Internal ID15089251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162308349..162327523hg38UCSC Ensembl
Innerchr6:162729381..162748555hg19UCSC Ensembl
Innerchr6:162649371..162668545hg18UCSC Ensembl
Innerchr6:162699792..162718966hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3819175
hg1919175
hg1819175
hg1719175
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)nssv699285
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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