A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969393



Internal ID18899202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:9900824..9901324hg38UCSC Ensembl
Outerchr19:10011500..10012000hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121968
Supporting Variants
SamplesKWS2
Known GenesOLFM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969393
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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