A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6137921



Internal ID337102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155380900..155386000hg38UCSC Ensembl
chrX:154610549..154615649hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg385101
hg195101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738201
Samples
Known GenesF8A1, F8A2, F8A3, H2AFB1, H2AFB2, H2AFB3, MIR1184-1, MIR1184-2, MIR1184-3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6137921
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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