A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316307



Internal ID20849386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9875366..9882072hg38UCSC Ensembl
chr1:9935424..9942130hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg386707
hg196707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065929
Samples
Known GenesCTNNBIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316307
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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