A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602424



Internal ID20975495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94603404..94603878hg38UCSC Ensembl
chr7:94232716..94233190hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161536
Samples
Known GenesSGCE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602424
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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