A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1073558



Internal ID15926744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:135737730..135772118hg38UCSC Ensembl
Innerchr6:136058868..136093256hg19UCSC Ensembl
Innerchr6:136100561..136134949hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3834389
hg1934389
hg1834389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604724
Supporting Variants
Samples
Known GenesMIR548H4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1073558
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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