A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601155



Internal ID20974226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121709771..121712908hg38UCSC Ensembl
chr7:121349825..121352962hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg383138
hg193138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151808
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601155
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