A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616473



Internal ID20989544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93482277..93483023hg38UCSC Ensembl
chr7:93111589..93112335hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161790
Samples
Known GenesCALCR, MIR653
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616473
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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