A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619041



Internal ID20992112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108355039..108410754hg38UCSC Ensembl
chr7:107995483..108051198hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3855716
hg1955716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147024
Samples
Known GenesNRCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619041
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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