A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153760



Internal ID20720800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40251762..40319261hg38UCSC Ensembl
chr7:40291361..40358860hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3867500
hg1967500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609716
Supporting Variants
Samples
Known GenesC7orf10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153760
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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