A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139014



Internal ID338198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155695000..156010500hg38UCSC Ensembl
chrX:154924661..155240165hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38315501
hg19315505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738244
Samples
Known GenesIL9R, SPRY3, VAMP7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139014
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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