A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602877



Internal ID20975948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95581788..95586720hg38UCSC Ensembl
chr7:95211100..95216032hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg384933
hg194933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162232
Samples
Known GenesPDK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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