A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159995



Internal ID20727035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92621588..92622063hg38UCSC Ensembl
chr7:92250902..92251377hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601059
Supporting Variants
Samples
Known GenesCDK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159995
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00103


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