A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607002



Internal ID21555307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115922270..115922270hg38UCSC Ensembl
chrX:115038603..115038603hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165256
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607002
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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