A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884285



Internal ID22659267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68286194..68286257hg38UCSC Ensembl
chr2:68513326..68513389hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396140
Samples
Known GenesCNRIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884285
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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