A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077838



Internal ID19315896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:22745172..22763473hg38UCSC Ensembl
chr17:22244499..22262800hg19UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg3818302
hg1918302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763978
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077838
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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