A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435290



Internal ID21397292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50969551..50972800hg38UCSC Ensembl
chr7:51037248..51040497hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg383250
hg193250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15748187
SamplesBTQ016
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435290
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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