A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151641



Internal ID20718681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133721314..133981447hg38UCSC Ensembl
chr7:133406067..133666200hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38260134
hg19260134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424445
Supporting Variants
Samples
Known GenesEXOC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151641
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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