A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2806967



Internal ID21252305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62229965..62230291hg38UCSC Ensembl
chr2:62457100..62457426hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13696015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2806967
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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