A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2801652



Internal ID21246990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60064308..60064308hg38UCSC Ensembl
chr1:60529980..60529980hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13690438
Samples
Known GenesC1orf87
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2801652
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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