A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768433



Internal ID19310130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37819823..37820224hg38UCSC Ensembl
chr6:37787599..37788000hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073550
Supporting Variants
SamplesKWP1
Known GenesZFAND3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768433
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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