A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3949259



Internal ID21369330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37330789..37331363hg38UCSC Ensembl
chr4:37332411..37332985hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15180551
SamplesHG002
Known GenesKIAA1239
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3949259
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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