A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077973



Internal ID19322394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140286645..140289146hg38UCSC Ensembl
chr4:141207799..141210300hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg382502
hg192502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765846
SamplesKWP1
Known GenesLOC100129858, SCOC
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077973
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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