A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069470



Internal ID18979142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34814571..34815772hg38UCSC Ensembl
chr10:35103499..35104700hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771456
SamplesKWP1
Known GenesPARD3, PARD3-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069470
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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