A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6137957



Internal ID337138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:127811000..127941400hg38UCSC Ensembl
chrX:126944979..127075379hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38130401
hg19130401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6137957
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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