A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2814910



Internal ID21260248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35136430..35137030hg38UCSC Ensembl
chr6:35104207..35104807hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13697248
Samples
Known GenesTCP11
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2814910
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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