A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475937



Internal ID253566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64516894..64517077hg38UCSC Ensembl
chr7:63977272..63977455hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16997159
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475937
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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