A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611731



Internal ID20984802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:118147601..118234750hg38UCSC Ensembl
chr7:117787655..117874804hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3887150
hg1987150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235739
Samples
Known GenesANKRD7, NAA38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611731
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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