A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2805498



Internal ID21250836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:180964369..180964369hg38UCSC Ensembl
chr2:181829096..181829096hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13684060
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2805498
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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