A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906569



Internal ID22681770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56432926..56434276hg38UCSC Ensembl
chr3:56466954..56468304hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg381351
hg191351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410639
Samples
Known GenesERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906569
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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