A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2799150



Internal ID21244488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43798138..43798138hg38UCSC Ensembl
chr19:44302290..44302290hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13695676
Samples
Known GenesLYPD5
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2799150
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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