A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617699



Internal ID20990770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92258779..92259883hg38UCSC Ensembl
chr7:91888093..91889197hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg381105
hg191105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159969
Samples
Known GenesANKIB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617699
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