A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157891



Internal ID20724931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64029689..64295968hg38UCSC Ensembl
chr7:63490067..63756346hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38266280
hg19266280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618015
Supporting Variants
Samples
Known GenesLINC01005, ZNF679, ZNF727, ZNF735
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157891
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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