A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768826



Internal ID19311274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110160217..110160658hg38UCSC Ensembl
chr13:110812564..110813005hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070197
Supporting Variants
SamplesKWP1
Known GenesCOL4A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768826
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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