A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2801265



Internal ID21246603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205603645..205603645hg38UCSC Ensembl
chr1:205572773..205572773hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13706919
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2801265
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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