A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950835



Internal ID21370904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6163188..6163479hg38UCSC Ensembl
chr19:6163199..6163490hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15177336
SamplesHG002
Known GenesACSBG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950835
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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