A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695018



Internal ID15084984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162587986..162594247hg38UCSC Ensembl
Innerchr6:163009018..163015279hg19UCSC Ensembl
Innerchr6:162929008..162935269hg18UCSC Ensembl
Innerchr6:162979429..162985690hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg386262
hg196262
hg186262
hg176262
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)nssv695018
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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