A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3931002



Internal ID21351071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2893191..2893191hg38UCSC Ensembl
chr6:2893425..2893425hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15201879
SamplesHG002
Known GenesSERPINB9
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3931002
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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