A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7002503



Internal ID10026057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46317046..46687628hg38UCSC Ensembl
Innerchr17:44394412..44764994hg19UCSC Ensembl
Innerchr17:41750187..42120174hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38370583
hg19370583
hg18369988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2762433
Supporting Variants
SamplesSW_1457
Known GenesARL17A, ARL17B, LRRC37A, LRRC37A2, NSF, NSFP1
MethodMerging
AnalysisTwo different algorithms (PennCNV and Birdseye) were applied to detect CNVs. Only congruent CNV events regarding direction of effect that were detected by both algorithms were merged using the outer borders of the event in a first step. In a second step only CNVs that were detected in at least two individuals were merged into a CNVR.
PlatformMerging
Comments
ReferenceVogler_et_al_2010
Pubmed ID21179565
Accession Number(s)essv7002503
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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