A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610632



Internal ID20983703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123150879..123155140hg38UCSC Ensembl
chr7:122790933..122795194hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg384262
hg194262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149444
Samples
Known GenesSLC13A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610632
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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