A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15205689



Internal ID21344490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45121761..45121761hg38UCSC Ensembl
chrX:44981006..44981006hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381149
hg191149
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938007
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15205689
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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