A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2797221



Internal ID21242559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79893803..79893952hg38UCSC Ensembl
chr17:77867602..77867751hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv138n137
Supporting Variantsnssv13689503
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2797221
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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