A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936179



Internal ID21356249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149239887..149240229hg38UCSC Ensembl
chr4:150161039..150161381hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15196520
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936179
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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