A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2813934



Internal ID21259272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106141590..106141685hg38UCSC Ensembl
chr7:105782036..105782131hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13699318
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2813934
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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