A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338540



Internal ID20996093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:76797442..76906262hg38UCSC Ensembl
chr2:77024568..77133388hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38108821
hg19108821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090400
Samples
Known GenesLRRTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338540
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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