A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830442



Internal ID22605377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70836612..70838111hg38UCSC Ensembl
chr1:71302295..71303794hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480721, nssv17481165
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830442
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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