A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613380



Internal ID21561685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140514521..140514521hg38UCSC Ensembl
chrX:139596686..139596686hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165822
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613380
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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