A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386268



Internal ID22444138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60623372..60624630hg38UCSC Ensembl
chr13:61197506..61198764hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg381259
hg191259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936853
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386268
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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