A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1072340



Internal ID18973570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20624408..20624597hg38UCSC Ensembl
chr19:20807214..20807403hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769169
SamplesKWP1
Known GenesZNF626
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1072340
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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