A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772899



Internal ID19310303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66021367..66021968hg38UCSC Ensembl
chr13:66595499..66596100hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070179
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772899
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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