A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162037



Internal ID20729077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93811345..93985532hg38UCSC Ensembl
chr7:93440657..93614844hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38174188
hg19174188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602545
Supporting Variants
Samples
Known GenesGNG11, GNGT1, TFPI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162037
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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