A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1072606



Internal ID19316798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39312573..39313874hg38UCSC Ensembl
chr21:40684499..40685800hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772388
SamplesKWP1
Known GenesBRWD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1072606
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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