A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075627



Internal ID19322221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65292845..65317055hg38UCSC Ensembl
chr9:42685399..42709600hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3824211
hg1924202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765535
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075627
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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