A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465931



Internal ID22523821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:74756025..74756112hg38UCSC Ensembl
chrX:73975860..73975947hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879856
Supporting Variants
Samples
Known GenesKIAA2022
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465931
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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