A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948213



Internal ID21368282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38076703..38076802hg38UCSC Ensembl
chr9:38076700..38076799hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15199697
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948213
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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