A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17572088



Internal ID21764131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91531691..91562291hg38UCSC Ensembl
chr7:91161006..91191606hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3830601
hg1930601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015054
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17572088
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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