A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771500



Internal ID18963200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184261211..184261912hg38UCSC Ensembl
chr3:183978999..183979700hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074644
Supporting Variants
SamplesKWP1
Known GenesCAMK2N2, ECE2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771500
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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