A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772699



Internal ID18964108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10690942..10696043hg38UCSC Ensembl
chr1:10750999..10756100hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg385102
hg195102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075150
Supporting Variants
SamplesKWP1
Known GenesCASZ1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772699
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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