A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229863



Internal ID20796904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65587481..65879642hg38UCSC Ensembl
chr7:65052394..65344629hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38292162
hg19292236
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609669
Supporting Variants
Samples
Known GenesCCT6P1, INTS4L2, LOC441242, SNORA22, VKORC1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229863
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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