A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13707552



Internal ID21229347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46275681..46275807hg38UCSC Ensembl
chrX:46135116..46135242hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2820380
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13707552
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.173077


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