A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950872



Internal ID17299746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:149525618..149535578hg38UCSC Ensembl
Outerchr1:144187001..144197000hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg389961
hg1910000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997245
SamplesBILGI_BIOE
Known GenesLOC100288142
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950872
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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