A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111768



Internal ID22021001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:111883165..111888950hg38UCSC Ensembl
chrX:111126393..111132178hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg385786
hg195786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640515
Samples
Known GenesTRPC5, TRPC5OS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111768
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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