A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617323



Internal ID20990394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27601201..27602300hg38UCSC Ensembl
chr7:27640820..27641919hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157034
Samples
Known GenesHIBADH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617323
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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