A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232972



Internal ID20800012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73446147..73449292hg38UCSC Ensembl
chr6:74155870..74159015hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg383146
hg193146
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396971
Supporting Variants
Samples
Known GenesMB21D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232972
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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