A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975678



Internal ID22750613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141849653..141861514hg38UCSC Ensembl
chrX:140937439..140949300hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3811862
hg1911862
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515566
Samples
Known GenesMAGEC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975678
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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