A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772617



Internal ID19313094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2260372..2262373hg38UCSC Ensembl
chr4:2262099..2264100hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg382002
hg192002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073719
Supporting Variants
SamplesKWP1
Known GenesMXD4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772617
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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