A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360337



Internal ID22586006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101855065..101855065hg38UCSC Ensembl
chr10:103614822..103614822hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961284
Supporting Variants
Samples
Known GenesC10orf76
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360337
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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