A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2805315



Internal ID21250653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:118092802..118092948hg38UCSC Ensembl
chr2:118850378..118850524hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13692524
Samples
Known GenesINSIG2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2805315
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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