A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577008



Internal ID21769051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107073197..107073249hg38UCSC Ensembl
chr6:107394401..107394453hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004198
Supporting Variants
Samples
Known GenesBEND3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577008
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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