A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608827



Internal ID20981898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75551300..75552457hg38UCSC Ensembl
chr7:75180599..75181756hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381158
hg191158
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224828
Samples
Known GenesHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608827
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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