A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614294



Internal ID20987365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119461824..119462285hg38UCSC Ensembl
chr7:119101878..119102339hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151047
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614294
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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