A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18160729



Internal ID20727769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96470501..96548300hg38UCSC Ensembl
chr7:96099813..96177612hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3877800
hg1977800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619543
Supporting Variants
Samples
Known GenesC7orf76
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18160729
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00064


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