A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452743



Internal ID22510616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:62633057..62674216hg38UCSC Ensembl
chrX:61852527..61893686hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3841160
hg1941160
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868213
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452743
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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