A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771135



Internal ID19307943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213151575..213152176hg38UCSC Ensembl
chr2:214016299..214016900hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072491
Supporting Variants
SamplesKWP1
Known GenesIKZF2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771135
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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