A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2813906



Internal ID21259244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100962770..100962839hg38UCSC Ensembl
chr7:100554593..100554668hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3870
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13703393
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2813906
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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