A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2801638



Internal ID21246976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:57606186..57606186hg38UCSC Ensembl
chr1:58071858..58071858hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13683749
Samples
Known GenesDAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2801638
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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