A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346996



Internal ID21004549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9478003..9483906hg38UCSC Ensembl
chr2:9618132..9624035hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg385904
hg195904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092595
Samples
Known GenesIAH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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