A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2817090



Internal ID21262428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76414814..76414814hg38UCSC Ensembl
chr7:76044131..76044131hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38683
hg19683
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705404
Samples
Known GenesZP3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2817090
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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