A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2794206



Internal ID21239544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40529729..40531389hg38UCSC Ensembl
chr15:40821928..40823588hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381661
hg191661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13686526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2794206
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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