A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770263



Internal ID19309179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8610714..8611515hg38UCSC Ensembl
chr19:8675599..8676400hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071508
Supporting Variants
SamplesKWP1
Known GenesADAMTS10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770263
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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