A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641346



Internal ID21833393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:129738077..129742153hg38UCSC Ensembl
chrX:128872053..128876129hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg384077
hg194077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107031
Supporting Variants
Samples
Known GenesXPNPEP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641346
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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