A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431952



Internal ID21089505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148973001..148978300hg38UCSC Ensembl
chr7:148670093..148675392hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7169n223
Supporting Variantsnssv18153993
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431952
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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