A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13697740



Internal ID21219594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115698868..115698922hg38UCSC Ensembl
chrX:114933188..114933242hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819445
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13697740
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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