A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13709306



Internal ID21231087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49069209..49069209hg38UCSC Ensembl
chrX:48926861..48926861hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2820731
Supporting Variants
Samples
Known GenesCCDC120
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13709306
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.8125


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