A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819700



Internal ID21265038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67538278..67538607hg38UCSC Ensembl
chr9:65906803..65907106hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38330
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv367n137
Supporting Variantsnssv13709780
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819700
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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