A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437502



Internal ID21095055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94620962..94635865hg38UCSC Ensembl
chr10:96380719..96395622hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3814904
hg1914904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985276
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437502
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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