A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150169



Internal ID19201157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:69228468..69228551hg38UCSC Ensembl
Outerchr7:68693455..68693538hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003469
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150169
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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