A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344096



Internal ID21001649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75112070..75118950hg38UCSC Ensembl
chr2:75339196..75346076hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg386881
hg196881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090239
Samples
Known GenesTACR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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