A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012976



Internal ID21922319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173740041..173740092hg38UCSC Ensembl
chr5:173167044..173167095hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559492
Samples
Known GenesLOC101928136
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012976
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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