A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322289



Internal ID20855401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150721401..150736010hg38UCSC Ensembl
chr1:150693877..150708486hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3814610
hg1914610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052987
Samples
Known GenesCTSS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322289
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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