A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416988



Internal ID21074541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:126981338..126981870hg38UCSC Ensembl
chr7:126621392..126621924hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152643
Samples
Known GenesGRM8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416988
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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