A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613872



Internal ID20986943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44883901..44886000hg38UCSC Ensembl
chr7:44923500..44925599hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231063
Samples
Known GenesPURB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613872
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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