A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509601



Internal ID20882912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44179468..44186142hg38UCSC Ensembl
chr17:42256836..42263510hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg386675
hg196675
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181709
Samples
Known GenesASB16-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509601
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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