A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981525



Internal ID18270036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:73174453..73182162hg38UCSC Ensembl
Innerchr7:72588493..72596202hg19UCSC Ensembl
Innerchr7:72226429..72234138hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg387710
hg197710
hg187710
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2464009, nssv2464005, nssv2464004, nssv2464011, nssv2464010, nssv2464002, nssv2464003, nssv2464006, nssv2464008, nssv2464007
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGTF2IP1, LOC100093631
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981525
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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