A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340101



Internal ID20997654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60950608..60975336hg38UCSC Ensembl
chr2:61177743..61202471hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3824729
hg1924729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089448
Samples
Known GenesPUS10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340101
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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