A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112444



Internal ID22021677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:62483733..62484069hg38UCSC Ensembl
chrX:61703203..61703539hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646168
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112444
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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