A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765149



Internal ID18968954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211259457..211260158hg38UCSC Ensembl
chr1:211432799..211433500hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1068848
Supporting Variants
SamplesKWP1
Known GenesRCOR3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765149
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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