A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610263



Internal ID20983334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122816853..122822735hg38UCSC Ensembl
chr7:122456907..122462789hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg385883
hg195883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149407
Samples
Known GenesCADPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610263
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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