A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335656



Internal ID20993209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:227320780..227321838hg38UCSC Ensembl
chr2:228185496..228186554hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg381059
hg191059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087051
Samples
Known GenesLOC654841
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335656
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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