A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322657



Internal ID20855770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17294525..17306975hg38UCSC Ensembl
chr1:17621020..17633470hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3812451
hg1912451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053953
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322657
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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