A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476577



Internal ID254184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23222110..23225663hg38UCSC Ensembl
chr10:23511039..23514592hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg383554
hg193554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032201
Samples
Known GenesC10orf115
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476577
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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