A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074445



Internal ID18976273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1420119..1420720hg38UCSC Ensembl
chr1:1355499..1356100hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767725
SamplesKWP1
Known GenesANKRD65
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074445
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer