A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17635987



Internal ID21828034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41555013..41555114hg38UCSC Ensembl
chr20:40183652..40183753hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056424
Supporting Variants
Samples
Known GenesCHD6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17635987
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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