A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068297



Internal ID18977240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33203668..33203996hg38UCSC Ensembl
chr10:33492596..33492924hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766440
SamplesKWP1
Known GenesNRP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1068297
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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