A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011422



Internal ID21920765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98584527..98685084hg38UCSC Ensembl
chr5:97920231..98020788hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38100558
hg19100558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011422
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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