A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100542



Internal ID22009775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:86155723..86162007hg38UCSC Ensembl
chrX:85410727..85417011hg19UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg386285
hg196285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647135
Samples
Known GenesDACH2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100542
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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