A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13708154



Internal ID21229947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102611780..102611780hg38UCSC Ensembl
chr7:102252227..102252227hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2815078
Supporting Variants
Samples
Known GenesRASA4, RASA4B
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13708154
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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