A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13710164



Internal ID21231938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136999977..137000280hg38UCSC Ensembl
chrX:136082136..136082439hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2820215
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13710164
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.383333


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