A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762132



Internal ID19310070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101097923..101098424hg38UCSC Ensembl
chr6:101545799..101546300hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073576
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762132
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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