A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872877



Internal ID22647819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37010042..37010293hg38UCSC Ensembl
chrX:37028115..37028366hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468569
Samples
Known GenesFAM47C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872877
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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