A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17440074



Internal ID22497944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:146101763..146101890hg38UCSC Ensembl
chrX:145183281..145183408hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875201
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17440074
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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