A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2805846



Internal ID21251184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:181491246..181491560hg38UCSC Ensembl
chr2:182355973..182356287hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13710053
Samples
Known GenesITGA4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2805846
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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