A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431226



Internal ID21088779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:127160402..127160695hg38UCSC Ensembl
chr7:126800456..126800749hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152667
Samples
Known GenesGRM8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431226
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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