A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071537



Internal ID19320195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45251241..45251742hg38UCSC Ensembl
chr19:45754499..45755000hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766127
SamplesKWP1
Known GenesMARK4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071537
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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