A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077365



Internal ID19321450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97193562..97232063hg38UCSC Ensembl
chr2:97859299..97897800hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3838502
hg1938502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767750
SamplesKWP1
Known GenesANKRD36
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077365
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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