A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335102



Internal ID20868293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8120801..8130700hg38UCSC Ensembl
chr1:8180861..8190760hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg389900
hg199900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv39n223
Supporting Variantsnssv18064202
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335102
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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