A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648231



Internal ID21840278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71255084..71255140hg38UCSC Ensembl
chrX:70474934..70474990hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110316
Supporting Variants
Samples
Known GenesBCYRN1, ZMYM3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648231
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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