A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880990



Internal ID22655961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:863087..962195hg38UCSC Ensembl
chr1:798467..897575hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3899109
hg1999109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375324
Samples
Known GenesFAM41C, KLHL17, LOC100130417, NOC2L, SAMD11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880990
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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