A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3927019



Internal ID21347090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113830487..113830637hg38UCSC Ensembl
chr13:114533460..114533610hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15183640
SamplesHG002
Known GenesGAS6, GAS6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3927019
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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