A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772529



Internal ID18967068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104641841..104642642hg38UCSC Ensembl
chr10:106401599..106402400hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069073
Supporting Variants
SamplesKWP1
Known GenesSORCS3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772529
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