A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13690255



Internal ID21212108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15611580..15611657hg38UCSC Ensembl
chr2:15751704..15751781hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2805784
Supporting Variants
Samples
Known GenesDDX1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13690255
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.354839


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