A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030927



Internal ID18773459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161715127..161956796hg38UCSC Ensembl
Innerchr6:162136159..162377828hg19UCSC Ensembl
Innerchr6:162056149..162297818hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38241670
hg19241670
hg18241670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6169n100
Supporting Variantsnssv3654534
Samples
Known GenesPARK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030927
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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