A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984776



Internal ID18858172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:39342160..39342660hg38UCSC Ensembl
Outerchr19:39832800..39833300hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126522
Supporting Variants
SamplesKWS1
Known GenesSAMD4B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984776
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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