A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610787



Internal ID20983858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29629301..29657700hg38UCSC Ensembl
chr7:29668917..29697316hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3828400
hg1928400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6632n223
Supporting Variantsnssv18232997
Samples
Known GenesLOC646762
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610787
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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