A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287273



Internal ID20496491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92339141..92339256hg38UCSC Ensembl
chr7:91968455..91968570hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739856
Supporting Variants
Samples
Known GenesANKIB1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287273
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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