A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077316



Internal ID19318619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7564636..7566037hg38UCSC Ensembl
chr10:7606599..7608000hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770222
SamplesKWP1
Known GenesITIH5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077316
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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