A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769169



Internal ID18963687
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 StatusS
Merged Variantsnsv1072340
Supporting Variants
SamplesKWP1
Known GenesZNF626
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769169
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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