A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327578



Internal ID20860718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32213336..32219559hg38UCSC Ensembl
chr1:32678937..32685160hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg386224
hg196224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060439
Samples
Known GenesDCDC2B, TMEM234
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327578
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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