A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13710184



Internal ID21231957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56776936..56777274hg38UCSC Ensembl
chr1:57242609..57242947hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801984
Supporting Variants
Samples
Known GenesC1orf168
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13710184
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.890625


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