A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349301



Internal ID21006854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9556829..9558164hg38UCSC Ensembl
chr2:9696958..9698293hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381336
hg191336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092598
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349301
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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