A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13711512



Internal ID21233268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71071575..71071575hg38UCSC Ensembl
chrX:70291425..70291425hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2820588
Supporting Variants
Samples
Known GenesSNX12
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13711512
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.483333


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