A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607087



Internal ID20980158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27538514..27539208hg38UCSC Ensembl
chr7:27578133..27578827hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38695
hg19695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157029
Samples
Known GenesHIBADH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607087
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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