A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335196



Internal ID20868388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:170948947..170949668hg38UCSC Ensembl
chr1:170918088..170918809hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053428
Samples
Known GenesMROH9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335196
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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