A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607692



Internal ID21555997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31345567..31345567hg38UCSC Ensembl
chr1:31818414..31818414hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064602
SamplesNA19239
Known GenesZCCHC17
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607692
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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