A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435282



Internal ID21397284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46884116..46894304hg38UCSC Ensembl
chr7:46923714..46933902hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3810189
hg1910189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15747173, nssv15750351
SamplesBTQ038, BTQ016
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435282
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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