A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344197



Internal ID21001750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27468101..27473700hg38UCSC Ensembl
chr2:27690968..27696567hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085706
Samples
Known GenesIFT172
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344197
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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