A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074817



Internal ID19316999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16989624..16989680hg38UCSC Ensembl
chr5:16989733..16989789hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765889
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074817
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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