A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076156



Internal ID18978896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15684104..15684705hg38UCSC Ensembl
chr1:16010599..16011200hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762740
SamplesKWP1
Known GenesPLEKHM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076156
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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