A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444286



Internal ID21101839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32504208..32508997hg38UCSC Ensembl
chr10:32793136..32797925hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg384790
hg194790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980065
Samples
Known GenesCCDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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