A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981145



Internal ID19212768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:39890075..39890876hg38UCSC Ensembl
Outerchr19:40396400..40397200hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38802
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118830
Supporting Variants
SamplesKWS1
Known GenesFCGBP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981145
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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