A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350456



Internal ID21008009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:180526045..180527846hg38UCSC Ensembl
chr2:181390772..181392573hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081083
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350456
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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