A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884992



Internal ID22659976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20122136..20123135hg38UCSC Ensembl
chr17:20025449..20026448hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476164
Samples
Known GenesSPECC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884992
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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