A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603920



Internal ID20976991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124661241..124749652hg38UCSC Ensembl
chr7:124301295..124389706hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3888412
hg1988412
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234215
Samples
Known GenesGPR37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603920
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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