A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607029



Internal ID20980100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100055430..100059992hg38UCSC Ensembl
chr7:99653053..99657615hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg384563
hg194563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147675
Samples
Known GenesZSCAN21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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