A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv171n137



Internal ID22812791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10200391..10200576hg38UCSC Ensembl
chr2:10340517..10340702hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv2804923, nsv2805092
Samples
Known GenesC2orf48
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)dgv171n137
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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