A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115763



Internal ID18929407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:152401615..152416415hg38UCSC Ensembl
Outerchr7:152098700..152113500hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3814801
hg1914801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3703n106
Supporting Variantsnssv3977570
SamplesKWS2
Known GenesKMT2C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115763
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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