A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074953



Internal ID19322126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109483096..109483697hg38UCSC Ensembl
chr6:109804299..109804900hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769825
SamplesKWP1
Known GenesZBTB24
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074953
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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