A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000527



Internal ID16946793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:206777431..206777579hg38UCSC Ensembl
Outerchr1:206950776..206950924hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv956206
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000527
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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