A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032838



Internal ID19122060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:144657368..144788985hg38UCSC Ensembl
Innerchr6:144978504..145110121hg19UCSC Ensembl
Innerchr6:145020197..145151814hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38131618
hg19131618
hg18131618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749557
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)nsv1032838
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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