A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154765



Internal ID20721805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17886982..17887366hg38UCSC Ensembl
chr7:17926605..17926989hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616791
Supporting Variants
Samples
Known GenesSNX13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154765
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00107


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