A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001235



Internal ID21910578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155414468..155414527hg38UCSC Ensembl
chr7:155207163..155207222hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564523
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001235
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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