A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1072050



Internal ID15925236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110249531..110250438hg38UCSC Ensembl
Innerchr6:110570734..110571641hg19UCSC Ensembl
Innerchr6:110677427..110678334hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38908
hg19908
hg18908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604515
Supporting Variants
Samples
Known GenesMETTL24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1072050
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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