A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3932740



Internal ID21352810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182124895..182124956hg38UCSC Ensembl
chr4:183046048..183046109hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15195768
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3932740
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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