A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923946



Internal ID22699173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143419749..143420565hg38UCSC Ensembl
chr7:143116842..143117658hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445174
Samples
Known GenesEPHA1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923946
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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