A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329280



Internal ID20862431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:81869301..81870700hg38UCSC Ensembl
chr1:82334986..82336385hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063283
Samples
Known GenesLPHN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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