A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619072



Internal ID20992143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20297012..20297795hg38UCSC Ensembl
chr7:20336635..20337418hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38784
hg19784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156884
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619072
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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