A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103238



Internal ID22012471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:11653288..11653711hg38UCSC Ensembl
chrX:11671408..11671831hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38424
hg19424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640949
Samples
Known GenesARHGAP6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103238
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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