A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658001



Internal ID15047967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162078145..162085536hg38UCSC Ensembl
Innerchr6:162499177..162506568hg19UCSC Ensembl
Innerchr6:162419167..162426558hg18UCSC Ensembl
Innerchr6:162469588..162476979hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg387392
hg197392
hg187392
hg177392
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)nssv658001
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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