A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925102



Internal ID22700329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23141571..23142793hg38UCSC Ensembl
chr7:23181190..23182412hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381223
hg191223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441731
Samples
Known GenesKLHL7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925102
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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