A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619885



Internal ID20992956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123652021..123675559hg38UCSC Ensembl
chr7:123292075..123315613hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3823539
hg1923539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150092
Samples
Known GenesLMOD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619885
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