A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609780



Internal ID20982851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2712919..2713471hg38UCSC Ensembl
chr7:2752553..2753105hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157009
Samples
Known GenesAMZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609780
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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