A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462134



Internal ID21119687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60212553..60299681hg38UCSC Ensembl
chr11:59980026..60067154hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3887129
hg1987129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1201n223
Supporting Variantsnssv17992492
Samples
Known GenesMS4A4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462134
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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