A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027905



Internal ID21937248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47632308..47633588hg38UCSC Ensembl
chr11:47653860..47655140hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381281
hg191281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587119
Samples
Known GenesMTCH2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027905
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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