A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951384



Internal ID16953571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:100100678..100114877hg38UCSC Ensembl
Outerchr7:99698301..99712500hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3814200
hg1914200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998550
SamplesBILGI_BIOE
Known GenesAP4M1, MCM7, TAF6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951384
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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