A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14353458



Internal ID22266096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:125321662..125321725hg38UCSC Ensembl
chrX:124455511..124455574hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206938
Supporting Variants
SamplesNA19238
Known GenesLOC100129520
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14353458
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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