A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909885



Internal ID22685095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20170675..20171226hg38UCSC Ensembl
chr7:20210298..20210849hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438656
Samples
Known GenesMACC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909885
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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