A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345652



Internal ID21003205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:73150725..73155762hg38UCSC Ensembl
chr2:73377853..73382890hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg385038
hg195038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089703
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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