A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476631



Internal ID254238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156901454..156907390hg38UCSC Ensembl
chr7:156694148..156700084hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg385937
hg195937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17005983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476631
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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