A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999818



Internal ID16946084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35134797..35153797hg38UCSC Ensembl
Outerchr19:35625701..35644700hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3819001
hg1919000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953282
Supporting Variants
SamplesBILGI_BIOE
Known GenesFXYD1, FXYD7, LGI4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999818
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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