A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410176



Internal ID22468046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40894355..40894355hg38UCSC Ensembl
chr4:40896372..40896372hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5966470
Supporting Variants
Samples
Known GenesAPBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410176
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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