A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15200167



Internal ID21338963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1638902..1641373hg38UCSC Ensembl
chrX:1757795..1760266hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg382472
hg192472
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3941699
Supporting Variants
SamplesHG002
Known GenesASMT
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15200167
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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