A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009998



Internal ID21919341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113259088..113263245hg38UCSC Ensembl
chr7:112899143..112903300hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg384158
hg194158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557538
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009998
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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