A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769618



Internal ID19314917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:21673860..21675461hg38UCSC Ensembl
chr13:22247999..22249600hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071085
Supporting Variants
SamplesKWP1
Known GenesFGF9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769618
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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