A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2797673



Internal ID21243011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11509265..11509265hg38UCSC Ensembl
chr18:11509264..11509264hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13677526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2797673
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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