A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140846



Internal ID18922467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:134802123..134802178hg38UCSC Ensembl
Outerchr7:134486874..134486929hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3957900, nssv3975314
SamplesKWS2, KWS1
Known GenesCALD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140846
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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