A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950377



Internal ID17299251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:30908354..30908953hg38UCSC Ensembl
Outerchr1:31381201..31381800hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997116
SamplesBILGI_BIOE
Known GenesSDC3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950377
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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