A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417074



Internal ID21074627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131070670..131076802hg38UCSC Ensembl
chr7:130755429..130761561hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg386133
hg196133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154068
Samples
Known GenesLINC-PINT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417074
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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