A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17643547



Internal ID21835594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:114605987..114605987hg38UCSC Ensembl
chrX:113840443..113840443hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045735
Supporting Variants
Samples
Known GenesHTR2C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17643547
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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