A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12n206



Internal ID22755316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16483139..16951955hg38UCSC Ensembl
chr1:16809634..17278450hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38468817
hg19468817
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5559248, nsv5560911
Samples
Known GenesCROCC, CROCCP2, CROCCP3, ESPNP, LOC729574, MIR3675, MST1L, MST1P2, NBPF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv12n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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