A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415850



Internal ID195097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136217041..136219978hg38UCSC Ensembl
chrX:135299200..135302137hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg382938
hg192938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742533
Samples
Known GenesMAP7D3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415850
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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