A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873542



Internal ID22648490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31985609..31988755hg38UCSC Ensembl
chr20:30573412..30576558hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg383147
hg193147
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485292
Samples
Known GenesXKR7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873542
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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