A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495606



Internal ID20868800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15145301..15157000hg38UCSC Ensembl
chr17:15048618..15060317hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3811700
hg1911700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3005n223
Supporting Variantsnssv18033921
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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