A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917734



Internal ID22692954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29984731..29985361hg38UCSC Ensembl
chr7:30024347..30024977hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444025
Samples
Known GenesSCRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917734
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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