A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606364



Internal ID20979435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96364201..96365200hg38UCSC Ensembl
chr7:95993513..95994512hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160715
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606364
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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