A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103540



Internal ID22012773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:125321240..125321300hg38UCSC Ensembl
chrX:124455089..124455149hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647496
Samples
Known GenesLOC100129520
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103540
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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