A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2801083



Internal ID21246423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:181078275..181078275hg38UCSC Ensembl
chr1:181047411..181047411hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13678854, nssv13681992
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2801083
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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