A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629242



Internal ID21577547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28325553..28325553hg38UCSC Ensembl
chr6:28293330..28293330hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157736
SamplesNA19239
Known GenesZSCAN31
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629242
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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