A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490599



Internal ID267852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157421613..157432192hg38UCSC Ensembl
chr7:157214307..157224886hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3810580
hg1910580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17006943
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490599
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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