A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523485



Internal ID15104092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161788587..162333574hg38UCSC Ensembl
Innerchr6:162209619..162754606hg19UCSC Ensembl
Innerchr6:162129609..162674596hg18UCSC Ensembl
Innerchr6:162180030..162725017hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38544988
hg19544988
hg18544988
hg17544988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699251
Samples
Known GenesPARK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523485
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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