A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966291



Internal ID22741226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28147164..28147164hg38UCSC Ensembl
chr6:28114942..28114942hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447927
Samples
Known GenesZKSCAN8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966291
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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