A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15203443



Internal ID21342250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139101478..139101478hg38UCSC Ensembl
chr7:138786224..138786224hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3947357
Supporting Variants
SamplesHG002
Known GenesZC3HAV1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15203443
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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