A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322127



Internal ID20855237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145870320..145894282hg38UCSC Ensembl
chr1:145540794..145564763hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg3823963
hg1923970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052129
Samples
Known GenesANKRD35, ITGA10, LOC100288142, NBPF10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322127
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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