A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192007



Internal ID20759047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6628273..6869404hg38UCSC Ensembl
chr10:6670235..6911366hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38241132
hg19241132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442370
Supporting Variants
Samples
Known GenesLINC00706, LINC00707
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192007
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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