A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13710250



Internal ID21232019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6318735..6318735hg38UCSC Ensembl
chr19:6318746..6318746hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38680
hg19680
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2800368
Supporting Variants
Samples
Known GenesACER1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13710250
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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