A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615480



Internal ID20988551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73733501..73740200hg38UCSC Ensembl
chr7:73147831..73154530hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226664
Samples
Known GenesABHD11, LINC00035
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615480
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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