A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321009



Internal ID20854111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32368901..32370200hg38UCSC Ensembl
chr1:32834502..32835801hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060448
Samples
Known GenesBSDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321009
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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