A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368501



Internal ID22594170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122260973..122273514hg38UCSC Ensembl
chr10:124020488..124033029hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3812542
hg1912542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912545
Supporting Variants
Samples
Known GenesBTBD16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368501
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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