A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315877



Internal ID20848951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182944081..182947170hg38UCSC Ensembl
chr1:182913216..182916305hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg383090
hg193090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054385
Samples
Known GenesSHCBP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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