A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936232



Internal ID21356301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70227583..70227583hg38UCSC Ensembl
chr4:71093300..71093300hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200487
SamplesHG002
Known GenesFDCSP
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936232
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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