A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616613



Internal ID20989684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107689958..107690444hg38UCSC Ensembl
chr7:107330403..107330889hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146985
Samples
Known GenesSLC26A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616613
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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