A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923628



Internal ID22698855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:68434662..68435455hg38UCSC Ensembl
chr7:67899649..67900442hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435112
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923628
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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