A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366471



Internal ID22592140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127367265..127369418hg38UCSC Ensembl
chr10:129165529..129167682hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg382154
hg192154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926008
Supporting Variants
Samples
Known GenesDOCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366471
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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