A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070861



Internal ID19320977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2614495..2614631hg38UCSC Ensembl
chr18:2614494..2614630hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767758
SamplesKWP1
Known GenesNDC80
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070861
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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