A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946250



Internal ID22721737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76602713..76610396hg38UCSC Ensembl
chr17:74598795..74606478hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg387684
hg197684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371159
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946250
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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