A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112271



Internal ID22021506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63720813..63720946hg38UCSC Ensembl
chrX:62940693..62940826hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644218
Samples
Known GenesARHGEF9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112271
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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