A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966835



Internal ID22741770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:113961274..113961274hg38UCSC Ensembl
chrX:113204559..113204559hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966835
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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