A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950342



Internal ID16952529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:27392797..27410906hg38UCSC Ensembl
Outerchr1:27719301..27737400hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3818110
hg1918100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997107
SamplesBILGI_BIOE
Known GenesGPR3, WASF2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950342
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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