A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112337



Internal ID22021570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123864778..123864848hg38UCSC Ensembl
chrX:122998628..122998698hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639010
Samples
Known GenesXIAP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112337
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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