A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607813



Internal ID20980884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12487951..12499235hg38UCSC Ensembl
chr7:12527577..12538861hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3811285
hg1911285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150223
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607813
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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