A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762801



Internal ID19313406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7174480..7176881hg38UCSC Ensembl
chr17:7077799..7080200hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg382402
hg192402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077836
Supporting Variants
SamplesKWP1
Known GenesASGR1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762801
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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