A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221137



Internal ID20788177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73275286..73325685hg38UCSC Ensembl
chr6:73985009..74035408hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3850400
hg1950400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401326
Supporting Variants
Samples
Known GenesC6orf147, KHDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221137
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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