A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645936



Internal ID21837983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73967670..73967724hg38UCSC Ensembl
chrX:73187505..73187559hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110059
Supporting Variants
Samples
Known GenesJPX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645936
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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