A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607450



Internal ID20980521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64088181..64357899hg38UCSC Ensembl
chr7:63548559..63818277hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38269719
hg19269719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6857n223
Supporting Variantsnssv18157899
Samples
Known GenesZNF679, ZNF735, ZNF736
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607450
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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