A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486770



Internal ID22544685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61603817..61647896hg38UCSC Ensembl
chr20:60178873..60222952hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3844080
hg1944080
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874803
Supporting Variants
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486770
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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