A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395665



Internal ID21053218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:51594978..51601713hg38UCSC Ensembl
chr6:51459776..51466511hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg386736
hg196736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145065
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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