A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619102



Internal ID20992173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99472612..99481757hg38UCSC Ensembl
chr7:99070235..99079380hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg389146
hg199146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162422
Samples
Known GenesZNF789
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619102
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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