A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339831



Internal ID20997384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9205701..9207200hg38UCSC Ensembl
chr2:9345830..9347329hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092581
Samples
Known GenesASAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339831
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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