A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149070



Internal ID21466650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139100755..139100804hg38UCSC Ensembl
chr7:138785501..138785550hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570185
Supporting Variants
SamplesHG03065
Known GenesZC3HAV1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149070
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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