A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15205693



Internal ID21344494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45721206..45721206hg38UCSC Ensembl
chrX:45580443..45580443hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3933761
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15205693
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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