A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957068



Internal ID17305941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:130025014..130025149hg38UCSC Ensembl
Outerchr7:129664854..129664989hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001058
SamplesBILGI_BIOE
Known GenesZC3HC1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957068
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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