A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070871



Internal ID19324710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25348935..25352236hg38UCSC Ensembl
chr18:22928899..22932200hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383302
hg193302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771329
SamplesKWP1
Known GenesZNF521
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070871
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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