A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4170996



Internal ID11106848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73147935..73148169hg38UCSC Ensembl
chr17:71144074..71144308hg19UCSC Ensembl
chr17:68655669..68655903hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38235
hg19235
hg18235
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1404271
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4170996
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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