A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741224



Internal ID164890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:86558542..87176542hg38UCSC Ensembl
chrX:85813545..86431545hg19UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg38618001
hg19618001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138899
Supporting Variants
Samples
Known GenesDACH2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741224
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000418848


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