A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412970



Internal ID21070523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1993782..2006842hg38UCSC Ensembl
chr6:1994016..2007076hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3813061
hg1913061
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143167
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412970
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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