A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415821



Internal ID21073374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139028244..139033080hg38UCSC Ensembl
chr7:138712990..138717826hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg384837
hg194837
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233038
Samples
Known GenesZC3HAV1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415821
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