A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13711351



Internal ID21233110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120374826..120374826hg38UCSC Ensembl
chrX:119508681..119508681hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819771
Supporting Variants
Samples
Known GenesATP1B4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13711351
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.984375


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