A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107216



Internal ID22016449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48635955..48636020hg38UCSC Ensembl
chrX:48494343..48494408hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644125
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107216
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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