A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600703



Internal ID20973774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121563701..121569500hg38UCSC Ensembl
chr7:121203755..121209554hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220300
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600703
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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