A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109598



Internal ID22018831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155890516..155903747hg38UCSC Ensembl
chrX:155120179..155133411hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3813232
hg1913233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639039
Samples
Known GenesVAMP7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109598
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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