A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156801



Internal ID20723841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39664581..39665198hg38UCSC Ensembl
chr7:39704180..39704797hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613072
Supporting Variants
Samples
Known GenesRALA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156801
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0012


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