A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771063



Internal ID18964005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94773894..94774269hg38UCSC Ensembl
chr5:94109599..94109974hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074320
Supporting Variants
SamplesKWP1
Known GenesMCTP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771063
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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