A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604941



Internal ID20978012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99375374..99381140hg38UCSC Ensembl
chr7:98972997..98978763hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg385767
hg195767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162415
Samples
Known GenesARPC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604941
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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