A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352761



Internal ID22578430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61013102..61013696hg38UCSC Ensembl
chr10:62772860..62773454hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922510
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352761
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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