A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271330



Internal ID20480548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49114937..49114937hg38UCSC Ensembl
chrX:48971876..48971876hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731612
Supporting Variants
Samples
Known GenesGPKOW
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271330
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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