A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601558



Internal ID20974629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95310424..95338769hg38UCSC Ensembl
chr7:94939736..94968081hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3828346
hg1928346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161618
Samples
Known GenesPON1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601558
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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