A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601337



Internal ID20974408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23665501..23729800hg38UCSC Ensembl
chr7:23705120..23769419hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3864300
hg1964300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233180
Samples
Known GenesFAM221A, STK31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601337
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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