A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954825



Internal ID16957012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:15698506..15753805hg38UCSC Ensembl
Outerchr1:16025001..16080300hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3855300
hg1955300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003108
SamplesBILGI_BIOE
Known GenesPLEKHM2, SLC25A34, TMEM82
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954825
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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