A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2800798



Internal ID21246136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155700969..155700969hg38UCSC Ensembl
chr1:155670760..155670760hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13709135
Samples
Known GenesDAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2800798
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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