A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607936



Internal ID20981007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94528689..94529124hg38UCSC Ensembl
chr7:94158001..94158436hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161524
Samples
Known GenesCASD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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