A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025098



Internal ID19114316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162798971..162922526hg38UCSC Ensembl
Innerchr6:163220003..163343558hg19UCSC Ensembl
Innerchr6:163139993..163263548hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38123556
hg19123556
hg18123556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749610
Samples
Known GenesPACRG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025098
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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