A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2817490



Internal ID21262828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98510730..98510801hg38UCSC Ensembl
chr7:98140042..98140113hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13709761
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2817490
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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