A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157899



Internal ID20724939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64088181..64357899hg38UCSC Ensembl
chr7:63548559..63818277hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38269719
hg19269719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607450
Supporting Variants
Samples
Known GenesZNF679, ZNF735, ZNF736
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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