A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13703013



Internal ID21224832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:144923002..144923002hg38UCSC Ensembl
chrX:144004522..144004522hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2820127
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13703013
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.290323


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