A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2801237



Internal ID21246577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45497644..45497644hg38UCSC Ensembl
chr1:45963316..45963316hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13697907
Samples
Known GenesCCDC163P
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2801237
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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