A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503076



Internal ID20876327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16303717..16310662hg38UCSC Ensembl
chr17:16207031..16213976hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg386946
hg196946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034602
Samples
Known GenesPIGL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503076
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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