A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118113



Internal ID19276400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:31937699..31938399hg38UCSC Ensembl
Outerchr1:32403300..32404000hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv71n106
Supporting Variantsnssv3980333
SamplesKWS1
Known GenesPTP4A2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118113
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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