A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881696



Internal ID22656672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3951100..3952513hg38UCSC Ensembl
chr1:4011160..4012573hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg381414
hg191414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387438
Samples
Known GenesLOC728716
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881696
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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