A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078024



Internal ID18975550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71602914..71604515hg38UCSC Ensembl
chr7:71067899..71069500hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762762
SamplesKWP1
Known GenesWBSCR17
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078024
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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