A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642499



Internal ID21834546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:87663424..87663424hg38UCSC Ensembl
chrX:86918424..86918424hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050810
Supporting Variants
Samples
Known GenesKLHL4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642499
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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