A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2815078



Internal ID21260416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102611780..102611780hg38UCSC Ensembl
chr7:102252227..102252227hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13708154, nssv13697423
Samples
Known GenesRASA4, RASA4B
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2815078
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer