A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439121



Internal ID22496991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101166303..101166946hg38UCSC Ensembl
chrX:100421292..100421935hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872426
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439121
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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