A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811811



Internal ID21257149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61505654..61505654hg38UCSC Ensembl
chr5:60801481..60801481hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13702701
Samples
Known GenesZSWIM6
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811811
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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