A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765275



Internal ID18968200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4135365..4136066hg38UCSC Ensembl
chr6:4135599..4136300hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074367
Supporting Variants
SamplesKWP1
Known GenesECI2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765275
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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