A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434868



Internal ID21092421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128061286..128067080hg38UCSC Ensembl
chr7:127701338..127707132hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg385795
hg195795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152710
Samples
Known GenesSND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434868
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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