A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14350380



Internal ID22262502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42473387..42475078hg38UCSC Ensembl
chrX:42332639..42334330hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg381692
hg191692
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197675
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14350380
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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