A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601900



Internal ID20974971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:100509652..100511191hg38UCSC Ensembl
chr6:100957528..100959067hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg381540
hg191540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135772
Samples
Known GenesASCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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