A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008373



Internal ID21917716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:847743..847917hg38UCSC Ensembl
chr7:887380..887554hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571178
Samples
Known GenesSUN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008373
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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