A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2800516



Internal ID21245854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8449528..8449834hg38UCSC Ensembl
chr19:8514412..8514718hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13701364
Samples
Known GenesHNRNPM
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2800516
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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