A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15206128



Internal ID21344924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85911152..85911152hg38UCSC Ensembl
chrX:85166157..85166157hg19UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3953128
Supporting Variants
SamplesHG002
Known GenesCHM
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15206128
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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