A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004260



Internal ID21913603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77317484..77319029hg38UCSC Ensembl
chr7:76946801..76948346hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381546
hg191546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567383
Samples
Known GenesGSAP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004260
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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