A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5539739



Internal ID314626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75089238..75089289hg38UCSC Ensembl
chrX:74309073..74309124hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740784
Samples
Known GenesABCB7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5539739
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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