A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023014



Internal ID19112231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:144396827..144485555hg38UCSC Ensembl
Innerchr6:144717963..144806691hg19UCSC Ensembl
Innerchr6:144759656..144848384hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3888729
hg1988729
hg1888729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654455
Samples
Known GenesUTRN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023014
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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