A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607231



Internal ID20980302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86986369..87088179hg38UCSC Ensembl
chr7:86615685..86717495hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38101811
hg19101811
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234449
Samples
Known GenesKIAA1324L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607231
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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