A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034044



Internal ID20601084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10800201..10801300hg38UCSC Ensembl
chr17:10703518..10704617hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514220
Supporting Variants
Samples
Known GenesLINC00675, TMEM220-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034044
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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