A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970200



Internal ID22745135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119813592..119822291hg38UCSC Ensembl
chrX:118947555..118956254hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515260
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970200
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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