A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015631



Internal ID21924974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155886361..155886426hg38UCSC Ensembl
chr7:155679055..155679120hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567827
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015631
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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