A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455736



Internal ID22513613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119019779..119024094hg38UCSC Ensembl
chr10:120779291..120783606hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg384316
hg194316
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860573
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455736
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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