A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491344



Internal ID268585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74392083..74392558hg38UCSC Ensembl
chr7:73806413..73806888hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000973
Samples
Known GenesCLIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491344
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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