A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767575



Internal ID18959195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173370048..173371649hg38UCSC Ensembl
chr4:174291199..174292800hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074240
Supporting Variants
SamplesKWP1
Known GenesSAP30
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767575
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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