A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602160



Internal ID20975231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150302048..150305393hg38UCSC Ensembl
chr6:150623184..150626529hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg383346
hg193346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6450n223
Supporting Variantsnssv18141017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602160
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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