A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464285



Internal ID22522171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91439445..91456091hg38UCSC Ensembl
chr10:93199202..93215848hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3816647
hg1916647
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853396
Supporting Variants
Samples
Known GenesHECTD2, LOC100188947
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464285
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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