A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811232



Internal ID21256570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7230624..7230688hg38UCSC Ensembl
chr4:7232351..7232415hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13700020
Samples
Known GenesSORCS2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811232
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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