A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606637



Internal ID21798684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46735844..46735937hg38UCSC Ensembl
chr13:47309979..47310072hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038194
Supporting Variants
Samples
Known GenesLRCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606637
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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