A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412203



Internal ID21069756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42135414..42138427hg38UCSC Ensembl
chr6:42103152..42106165hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg383014
hg193014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143361
Samples
Known GenesC6orf132
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412203
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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