A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147063



Internal ID346256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:104603732..104609605hg38UCSC Ensembl
chrX:103848413..103854286hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg385874
hg195874
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737158
Samples
Known GenesIL1RAPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147063
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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