A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14350001



Internal ID22277156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:20094505..20094569hg38UCSC Ensembl
chrX:20112623..20112687hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3524889
Supporting Variants
SamplesNA19239
Known GenesMAP7D2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14350001
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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