A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070404



Internal ID18979288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39798786..39805013hg38UCSC Ensembl
chr17:37955039..37961266hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg386228
hg196228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764702
SamplesKWP1
Known GenesIKZF3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070404
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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