A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438950



Internal ID22496820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13413891..13418365hg38UCSC Ensembl
chr7:13453516..13457990hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg384475
hg194475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909728
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438950
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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