A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603798



Internal ID20976869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16195839..16231344hg38UCSC Ensembl
chr7:16235464..16270969hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3835506
hg1935506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152263
Samples
Known GenesISPD, ISPD-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603798
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