A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190634



Internal ID21329494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15350308..15350308hg38UCSC Ensembl
chr4:15351932..15351932hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3929676
Supporting Variants
SamplesHG002
Known GenesC1QTNF7
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190634
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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