A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434366



Internal ID22492236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139667882..139669310hg38UCSC Ensembl
chr7:139352628..139354056hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381429
hg191429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912713
Supporting Variants
Samples
Known GenesHIPK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434366
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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