A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152377



Internal ID20719417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135600188..136466331hg38UCSC Ensembl
chr7:135284936..136151079hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38866144
hg19866144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424183
Supporting Variants
Samples
Known GenesC7orf73, FAM180A, LUZP6, MTPN, NUP205, SLC13A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152377
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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