A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5472588



Internal ID250293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:273807..295043hg38UCSC Ensembl
chr7:313773..335009hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3821237
hg1921237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16992050
Samples
Known GenesLOC100288524
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5472588
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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