A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950335



Internal ID17299209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:25767010..25769809hg38UCSC Ensembl
Outerchr1:26093501..26096300hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997100
SamplesBILGI_BIOE
Known GenesMAN1C1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950335
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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