A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034389



Internal ID19123611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:82011852..82036882hg38UCSC Ensembl
Innerchr6:82721569..82746599hg19UCSC Ensembl
Innerchr6:82778288..82803318hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3825031
hg1925031
hg1825031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648880
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)nsv1034389
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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