A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342407



Internal ID20999960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75403126..75404457hg38UCSC Ensembl
chr2:75630252..75631583hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg381332
hg191332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090259
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342407
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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