A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453260



Internal ID22511134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124498930..124503486hg38UCSC Ensembl
chr10:126187499..126192055hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg384557
hg194557
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848560
Supporting Variants
Samples
Known GenesLHPP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453260
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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