A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2805784



Internal ID21251122
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 StatusM
Merged Variants
Supporting Variantsnssv13690255
Samples
Known GenesDDX1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2805784
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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