A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138965



Internal ID338149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155641418..155958181hg38UCSC Ensembl
chrX:154871079..155187846hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38316764
hg19316768
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738230
Samples
Known GenesSPRY3, VAMP7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138965
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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