A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103062



Internal ID22012295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:113109152..113113982hg38UCSC Ensembl
chrX:112352380..112357210hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg384831
hg194831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640307
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103062
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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