A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605147



Internal ID20978218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30366241..30366743hg38UCSC Ensembl
chr7:30405857..30406359hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155695
Samples
Known GenesZNRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605147
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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