A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14349925



Internal ID22277068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15799471..15800206hg38UCSC Ensembl
chrX:15817594..15818329hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38736
hg19736
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3198276
Supporting Variants
SamplesNA19239
Known GenesZRSR2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14349925
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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