A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463680



Internal ID22521566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91479966..91483219hg38UCSC Ensembl
chr10:93239723..93242976hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg383254
hg193254
Variant TypeOTHER copy number variation
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854451
Supporting Variants
Samples
Known GenesHECTD2, LOC100188947
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463680
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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