A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225415



Internal ID20792455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65664001..65910200hg38UCSC Ensembl
chr7:65128948..65375187hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38246200
hg19246240
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611499
Supporting Variants
Samples
Known GenesCCT6P1, INTS4L2, LOC441242, SNORA22, VKORC1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225415
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.05582


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