A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335441



Internal ID20868633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9908601..9910700hg38UCSC Ensembl
chr1:9968659..9970758hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065977
Samples
Known GenesCTNNBIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335441
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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