A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115107



Internal ID19276085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:75030702..75030786hg38UCSC Ensembl
Outerchr8:75942937..75943021hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975406
SamplesKWS2
Known GenesCRISPLD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115107
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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