A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372775



Internal ID22598444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40737392..40737566hg38UCSC Ensembl
chr1:41203064..41203238hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877605
Supporting Variants
Samples
Known GenesNFYC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372775
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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