A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367425



Internal ID22593094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1628113..1629639hg38UCSC Ensembl
chr10:1670308..1671834hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381527
hg191527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916662
Supporting Variants
Samples
Known GenesADARB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367425
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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