A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955152



Internal ID16957339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:6613541..6615140hg38UCSC Ensembl
Outerchr1:6673601..6675200hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001667
SamplesBILGI_BIOE
Known GenesPHF13
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955152
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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