A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009756



Internal ID21919099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123996880..123997212hg38UCSC Ensembl
chr7:123636934..123637266hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569921
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009756
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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