A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577334



Internal ID21769377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92350641..92350713hg38UCSC Ensembl
chr7:91979955..91980027hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019890
Supporting Variants
Samples
Known GenesANKIB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577334
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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