A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070738



Internal ID19323964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3469506..3469640hg38UCSC Ensembl
chr16:3519506..3519640hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771327
SamplesKWP1
Known GenesNAA60
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070738
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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