A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913439



Internal ID22688655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74613241..74621550hg38UCSC Ensembl
chr7:74027561..74035865hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg388310
hg198305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442998
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913439
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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