A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17998882



Internal ID20565922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29861852..29869554hg38UCSC Ensembl
chr12:30014785..30022487hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg387703
hg197703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457104
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17998882
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00033


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