A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056977



Internal ID19146196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68082268..68183009hg38UCSC Ensembl
Innerchr17:66078392..66179150hg19UCSC Ensembl
Innerchr17:63590029..63690745hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38100742
hg19100759
hg18100717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3277n100
Supporting Variantsnssv3567752, nssv3567753
Samples
Known GenesLINC00674
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056977
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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