A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623617



Internal ID21571922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20729351..20729351hg38UCSC Ensembl
chr4:20730974..20730974hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136784
SamplesHG01114
Known GenesKCNIP4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623617
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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