A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261543



Internal ID20470761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71028775..71028975hg38UCSC Ensembl
chr6:71738478..71738678hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736366
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261543
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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