A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13706469



Internal ID21228265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:74568843..74568959hg38UCSC Ensembl
chrX:73788678..73788794hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2820905
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13706469
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.85


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