A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766621



Internal ID19305796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33204914..33292968hg38UCSC Ensembl
chr17:31531932..31619986hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3888055
hg1988055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072730
Supporting Variants
SamplesKWP1
Known GenesASIC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766621
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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