A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950069



Internal ID17298943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:61333374..61347473hg38UCSC Ensembl
Outerchr5:60629201..60643300hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3814100
hg1914100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997758
SamplesBILGI_BIOE
Known GenesZSWIM6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950069
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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