A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425721



Internal ID21083274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156968221..156970790hg38UCSC Ensembl
chr7:156760915..156763484hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg382570
hg192570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151489
Samples
Known GenesNOM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425721
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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