A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878007



Internal ID22652973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31349892..31362224hg38UCSC Ensembl
chr1:31822739..31835071hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg3812333
hg1912333
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379265
Samples
Known GenesZCCHC17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878007
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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