A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15205999



Internal ID21344799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47089406..47089406hg38UCSC Ensembl
chrX:46948805..46948805hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg381443
hg191443
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3944999
Supporting Variants
SamplesHG002
Known GenesRGN
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15205999
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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