A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017630



Internal ID21926973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61709792..61709846hg38UCSC Ensembl
chr5:61005619..61005673hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556587
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017630
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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