A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036725



Internal ID21946068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60388033..60388105hg38UCSC Ensembl
chr11:60155506..60155578hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584495
Samples
Known GenesMS4A7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036725
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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