A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702161



Internal ID15092127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162418657..162420385hg38UCSC Ensembl
Innerchr6:162839689..162841417hg19UCSC Ensembl
Innerchr6:162759679..162761407hg18UCSC Ensembl
Innerchr6:162810100..162811828hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381729
hg191729
hg181729
hg171729
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)nssv702161
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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