A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073588



Internal ID18971676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:130019754..130020455hg38UCSC Ensembl
chr6:130340899..130341600hg19UCSC Ensembl
Cytoband6q23.1
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771541
SamplesKWP1
Known GenesL3MBTL3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073588
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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