A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133962



Internal ID18906750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1378523..1378595hg38UCSC Ensembl
Outerchr10:1420718..1420790hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970292
SamplesKWS2
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133962
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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