A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606527



Internal ID20979598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90183301..90258000hg38UCSC Ensembl
chr7:89812615..89887314hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3874700
hg1974700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223730
Samples
Known GenesC7orf63, STEAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606527
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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