A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399701



Internal ID21057254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17504160..17506436hg38UCSC Ensembl
chr6:17504391..17506667hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382277
hg192277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143268
Samples
Known GenesCAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399701
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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