A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698178



Internal ID15088144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162296666..162483133hg38UCSC Ensembl
Innerchr6:162717698..162904165hg19UCSC Ensembl
Innerchr6:162637688..162824155hg18UCSC Ensembl
Innerchr6:162688109..162874576hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38186468
hg19186468
hg18186468
hg17186468
Variant TypeCNV gain
Copy Number
Allele State
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)nssv698178
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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