A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138739



Internal ID337923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37085488..37097488hg38UCSC Ensembl
chr8:30251757..30263765hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3812001
hg1912009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740086
Samples
Known GenesRBPMS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138739
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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