A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619026



Internal ID20992097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151156701..151383300hg38UCSC Ensembl
chr6:151477836..151704435hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38226600
hg19226600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217111
Samples
Known GenesAKAP12, ZBTB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619026
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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