A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078264



Internal ID18974537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:89219840..89219913hg38UCSC Ensembl
Outerchr7:88849154..88849227hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763022
SamplesKWP1
Known GenesZNF804B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078264
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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