A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4447295



Internal ID22113472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37437674..37438001hg38UCSC Ensembl
chr7:37477277..37477604hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761070
Samples
Known GenesELMO1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4447295
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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