A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025409



Internal ID19114627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:71466295..71495341hg38UCSC Ensembl
Innerchr6:72175998..72205044hg19UCSC Ensembl
Innerchr6:72232719..72261765hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3829047
hg1929047
hg1829047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3658811
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025409
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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