A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409955



Internal ID22467825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7756441..7756560hg38UCSC Ensembl
chr4:7758168..7758287hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896318
Supporting Variants
Samples
Known GenesAFAP1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409955
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