A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5948906



Internal ID22724368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40847410..40847410hg38UCSC Ensembl
chr7:40887009..40887009hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448460
Samples
Known GenesC7orf10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5948906
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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