A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951357



Internal ID17300231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:75724183..75738482hg38UCSC Ensembl
Outerchr7:75353501..75367800hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3814300
hg1914300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998527
SamplesBILGI_BIOE
Known GenesHIP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951357
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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