A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217752



Internal ID20784792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57048188..57091791hg38UCSC Ensembl
chr6:56912986..56956589hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3843604
hg1943604
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402424
Supporting Variants
Samples
Known GenesKIAA1586, ZNF451
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217752
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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