A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355278



Internal ID22580947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86722867..86723695hg38UCSC Ensembl
chr10:88482624..88483452hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38829
hg19829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5917506
Supporting Variants
Samples
Known GenesLDB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355278
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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