A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456600



Internal ID21114153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7353201..7354200hg38UCSC Ensembl
chr12:7505797..7506796hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002722
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456600
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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