A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150424



Internal ID18852370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:88890785..88892386hg38UCSC Ensembl
Outerchr7:88520099..88521700hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003722
SamplesKWB1
Known GenesZNF804B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150424
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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