A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605243



Internal ID20978314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45430868..45431357hg38UCSC Ensembl
chr7:45470467..45470956hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155054
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605243
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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