A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501814



Internal ID20875051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15761901..15794600hg38UCSC Ensembl
chr17:15665215..15697914hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3832700
hg1932700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3012n223
Supporting Variantsnssv18034560
Samples
Known GenesCDRT15P2, MEIS3P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501814
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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