A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17595706



Internal ID21787749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88745942..88785661hg38UCSC Ensembl
chr11:88479110..88518829hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3839720
hg1939720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040420
Supporting Variants
Samples
Known GenesGRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17595706
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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