A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070426



Internal ID18973535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2138269..2138970hg38UCSC Ensembl
chr11:2159499..2160200hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765166
SamplesKWP1
Known GenesIGF2, INS-IGF2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070426
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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