A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913231



Internal ID22688447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142138278..142138346hg38UCSC Ensembl
chr7:141838078..141838146hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432100
Samples
Known GenesLOC93432
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913231
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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