A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101400



Internal ID22010633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:147043302..147053446hg38UCSC Ensembl
chrX:146124820..146134964hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3810145
hg1910145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649356
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101400
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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