A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434835



Internal ID21092388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155804901..155805600hg38UCSC Ensembl
chr7:155597595..155598294hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151415
Samples
Known GenesSHH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434835
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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