A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654097



Internal ID15044063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162078145..162086658hg38UCSC Ensembl
Innerchr6:162499177..162507690hg19UCSC Ensembl
Innerchr6:162419167..162427680hg18UCSC Ensembl
Innerchr6:162469588..162478101hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg388514
hg198514
hg188514
hg178514
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)nssv654097
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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