A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500948



Internal ID20874178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44179502..44186079hg38UCSC Ensembl
chr17:42256870..42263447hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg386578
hg196578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035828
Samples
Known GenesASB16-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500948
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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