A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347805



Internal ID21005358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6235173..6236907hg38UCSC Ensembl
chr2:6375305..6377039hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg381735
hg191735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089155
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347805
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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