A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476894



Internal ID254493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29140877..29141086hg38UCSC Ensembl
chr7:29180493..29180702hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994647
Samples
Known GenesCPVL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476894
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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