A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943433



Internal ID22718882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6957928..6986474hg38UCSC Ensembl
chr17:6861247..6889793hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3828547
hg1928547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386054
Samples
Known GenesLOC100506713
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943433
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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