A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012800



Internal ID21922143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76885573..76885649hg38UCSC Ensembl
chr5:76181398..76181474hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543306
Samples
Known GenesS100Z
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012800
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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