A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765355



Internal ID19306786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110496551..110496722hg38UCSC Ensembl
chr13:111148898..111149069hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070614
Supporting Variants
SamplesKWP1
Known GenesCOL4A2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765355
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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