A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506406



Internal ID22564353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39037202..39047274hg38UCSC Ensembl
chr7:39076802..39086874hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3810073
hg1910073
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846596
Supporting Variants
Samples
Known GenesPOU6F2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506406
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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