A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603047



Internal ID20976118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123052736..123053079hg38UCSC Ensembl
chr6:123373881..123374224hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137429
Samples
Known GenesCLVS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603047
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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