A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763564



Internal ID19308556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38228059..38229760hg38UCSC Ensembl
chr19:38718699..38720400hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381702
hg191702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072349
Supporting Variants
SamplesKWP1
Known GenesDPF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763564
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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