A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17649288



Internal ID21841335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48609355..48609456hg38UCSC Ensembl
chrX:48467743..48467844hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112563
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17649288
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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