A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747747



Internal ID21385625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36958252..36959924hg38UCSC Ensembl
chr1:37423853..37425525hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381673
hg191673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433123
Supporting Variants
SamplesBTQ055
Known GenesGRIK3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747747
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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