A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958774



Internal ID22733833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36337098..36337098hg38UCSC Ensembl
chr7:36376707..36376707hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445769
Samples
Known GenesKIAA0895
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958774
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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