A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434880



Internal ID21092433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156588801..156655500hg38UCSC Ensembl
chr7:156381495..156448194hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3866700
hg1966700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219608
Samples
Known GenesC7orf13, LINC01006, RNF32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434880
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer