A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156627



Internal ID22087028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2570769..2674723hg38UCSC Ensembl
Outerchr7:2558569..2681714hg38UCSC Ensembl
Innerchr7:2610403..2714357hg19UCSC Ensembl
Outerchr7:2598203..2721348hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38123146
hg19123146
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4023020
Samples
Known GenesAMZ1, IQCE, TTYH3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156627
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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