A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103758



Internal ID22012991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140299815..140299901hg38UCSC Ensembl
chrX:139381980..139382066hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638708
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103758
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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