A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647061



Internal ID21839108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:39664022..39667722hg38UCSC Ensembl
chrX:39523276..39526976hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg383701
hg193701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112356
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647061
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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