A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913597



Internal ID22688813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120166520..120167796hg38UCSC Ensembl
chr7:119806574..119807850hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg381277
hg191277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430718
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913597
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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