A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609897



Internal ID20982968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111080001..111081300hg38UCSC Ensembl
chr7:110720057..110721356hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148505
Samples
Known GenesIMMP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609897
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