A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352214



Internal ID22139850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:74162806..74163301hg38UCSC Ensembl
chrX:73382641..73383136hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3205746
Supporting Variants
SamplesHG00513
Known GenesFTX
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352214
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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