A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458744



Internal ID22516627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64785088..64842361hg38UCSC Ensembl
chrX:64004968..64062241hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3857274
hg1957274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5883030
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458744
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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