A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619088



Internal ID20992159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95403091..95405749hg38UCSC Ensembl
chr7:95032403..95035061hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg382659
hg192659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161628
Samples
Known GenesPON2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619088
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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