A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701835



Internal ID15091801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162425998..162562811hg38UCSC Ensembl
Innerchr6:162847030..162983843hg19UCSC Ensembl
Innerchr6:162767020..162903833hg18UCSC Ensembl
Innerchr6:162817441..162954254hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38136814
hg19136814
hg18136814
hg17136814
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)nssv701835
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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