A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648875



Internal ID21840922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30663988..30663988hg38UCSC Ensembl
chrX:30682105..30682105hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050161
Supporting Variants
Samples
Known GenesGK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648875
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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