A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644901



Internal ID21836948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119664727..119664792hg38UCSC Ensembl
chrX:118798690..118798755hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109496
Supporting Variants
Samples
Known GenesSEPT6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644901
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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