A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070267



Internal ID18976796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40440200..40441701hg38UCSC Ensembl
chr15:40732399..40733900hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381502
hg191502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768761
SamplesKWP1
Known GenesBAHD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070267
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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