A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075979



Internal ID18971718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3675081..3675361hg38UCSC Ensembl
chr1:3591645..3591925hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764110
SamplesKWP1
Known GenesTP73
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075979
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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