A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617037



Internal ID21565342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65772967..65772967hg38UCSC Ensembl
chrX:64992809..64992809hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168259
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617037
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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