A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613624



Internal ID20986695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97117714..97118150hg38UCSC Ensembl
chr7:96747026..96747462hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160780
Samples
Known GenesACN9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613624
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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