A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950792



Internal ID16952979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:2418066..2544866hg38UCSC Ensembl
Outerchr7:2457701..2584500hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38126801
hg19126800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997596
SamplesBILGI_BIOE
Known GenesBRAT1, CHST12, LFNG, LOC101927181, MIR4648
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950792
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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