A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768766



Internal ID19305419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110635837..110647830hg38UCSC Ensembl
chr1:111178459..111190452hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3811994
hg1911994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076676
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768766
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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