A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324840



Internal ID20857969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60019201..60021000hg38UCSC Ensembl
chr1:60484873..60486672hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062035
Samples
Known GenesC1orf87
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324840
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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