A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262807



Internal ID20472025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76699612..76699812hg38UCSC Ensembl
chr5:75995437..75995637hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734255
Supporting Variants
Samples
Known GenesIQGAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262807
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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