A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068666



Internal ID19326756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6814502..6814557hg38UCSC Ensembl
chr10:6856464..6856519hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772924
SamplesKWP1
Known GenesLINC00707
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1068666
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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