A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613018



Internal ID20986089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37244581..37256940hg38UCSC Ensembl
chr7:37284186..37296545hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3812360
hg1912360
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236405
Samples
Known GenesELMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613018
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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