A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485156



Internal ID262553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158774123..159247996hg38UCSC Ensembl
chr7:158566814..159040686hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38473874
hg19473873
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17007027
Samples
Known GenesESYT2, LINC00689, VIPR2, WDR60
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485156
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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