A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17448932



Internal ID22506802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103078713..103108188hg38UCSC Ensembl
chr7:102719160..102748635hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3829476
hg1929476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920773
Supporting Variants
Samples
Known GenesARMC10, NAPEPLD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17448932
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer